EU regulators have indicated they may take regulatory action if a negative overall survival (OS) trend is confirmed during the second interim analysis of Aveo Pharmaceuticals Inc.’s ongoing TIVO-3 study of its VEGFR tyrosine kinase inhibitor, tivozanib, in heavily pre-treated advanced or metastatic renal cell carcinoma, planned for August 2019.
The possibility of EU regulatory action is noted by Aveo in an SEC filing for a proposed $25m public offering...



![Spotlight On RDCs, AOCs As Leading Novel Bioconjugates[Updated]](https://web.insights.norstella-labs.com/resizer/v2/3M7ZAWZOBNK7NG4A4WDOIFG6DU.jpg?smart=true&auth=392a1fdb3cfacb29445720c412410e598dbcc5f90f14857652cd498bd0faa0fb&width=400&height=225)

